METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial bone model
2026-03-05
METICULY COMPANY LIMITED
GUDID#
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial drawing guide
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial drawing guide and bone model
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region (advanced design) non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant S non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant M non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant L non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant XL non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region S non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region M non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region L non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region XL non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial bone model
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial drawing guide
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific surgical assisting kit (SAK): Cranial drawing guide and bone model
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant (advanced design) non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region (advanced design) non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant S non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant M non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant L non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant XL non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region S non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region M non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region L non-sterile
2026-03-05
METICULY Patient-specific titanium mesh implant - METICULY Patient-specific titanium mesh implant with orbital region XL non-sterile
2026-03-05
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Orbital Mesh non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Orbital Mesh S non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Facial Mesh S non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Facial Mesh M non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Facial Mesh L non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - METICULY Patient-specific titanium maxillofacial mesh implant : Facial Mesh XL non-sterile
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
METICULY Patient-specific titanium maxillofacial mesh implant - The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
2024-07-31
Meticuly - Meticuly’s patient-specific titanium mesh implant is a device designed individually to replace each patient’s bony voids in the cranial and/or craniofacial skeleton. The craniofacial skeleton comprises of frontal bone, temporal bone, occipital bone, parietal bone, sphenoid bone, supraorbital process, vomer. This patient-specific device is intended to be used with titanium screws. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion). The surgeon approves the design of the mesh implant prior to fabrication of the implant device.
2023-11-17
Meticuly - Meticuly’s patient-specific titanium mesh implant is a device designed individually to replace each patient’s bony voids in the cranial and/or craniofacial skeleton. The craniofacial skeleton comprises of frontal bone, temporal bone, occipital bone, parietal bone, sphenoid bone, supraorbital process, vomer. This patient-specific device is intended to be used with titanium screws. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion). The surgeon approves the design of the mesh implant prior to fabrication of the implant device.
2023-11-08
Meticuly - Meticuly’s patient-specific titanium mesh implant is a device designed individually to replace each patient’s bony voids in the cranial and/or craniofacial skeleton. The craniofacial skeleton comprises of frontal bone, temporal bone, occipital bone, parietal bone, sphenoid bone, supraorbital process, vomer. This patient-specific device is intended to be used with titanium screws. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion). The surgeon approves the design of the mesh implant prior to fabrication of the implant device.
2023-11-08